Reducing Intraoperative ESKAPE Transmission Through Use of a Personal Hand Hygiene System
Part of paid clinical trials in Portland, Oregon.
- Sponsor
- Oregon Health and Science University
- Study ID
- NCT04900298
- Status
- Recruiting
Conditions
- Cross Infection
- Surgical Wound Infection
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - 99 Years
- Healthy Volunteers
- Not accepted
Interventions
- SafeHaven Automated Hand Hygiene Device — DEVICEAnesthesia providers in the intervention arm will be given a personal hand hygiene device, containing 64% ethyl alcohol, which provides actionable real-time performance feedback. The personalized device will be affixed to the provider's waist and will remain there for use throughout the perioperative period. Performance feedback is given to the anesthesia provider in real time with the number of personal hand hygiene events and an hourly hand hygiene rate, which is displayed on the device. Devices will be handed out to participating providers in the preoperative bay and retrieved in the post-anesthesia care unit upon case completion.
Study Details
The investigators hypothesize that the use of a personal hand hygiene system (SafeHavenTM) by anesthesia providers in the adult operating room, combined with a novel infectious pathogen tracking system (OR PathTrac) will decrease participant exposure to pathologic bacteria in the adult operating room.
Key Dates
- Start date
- Jan 1, 2022
- Status verified
- Jun 2024
- Primary completion
- Dec 31, 2025
- Completion
- Jun 30, 2026
Study Design
- Enrollment
- 40 participants (estimated)
- Allocation
- NON_RANDOMIZED
- Intervention model
- SEQUENTIAL
- Primary purpose
- PREVENTION
Arms
- Experimental: Intervention ArmUse of SafeHaven hand hygiene system in the operating room
- No Intervention: Control ArmStandard of care hand hygiene
Primary Outcome Measure
Number of ESKAPE (Enterococcus, S. Aureus, Klebsiella, Acinetobacter, Pseudomonas, and Enterobacter spp.) reservoirs identified using microbial culture collection kits [ Time Frame: Perioperative Time, typically less than 12 hours ]
Central Contacts
- Brandon M Togioka, MD503-494-4572
- Sydney Rose, MD503-494-1358
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| Oregon Health and Science University | Portland | Oregon | 97239 | Sarah Feller Brandon M Togioka, MD (PRINCIPAL_INVESTIGATOR) Sydney Rose, MD (SUB_INVESTIGATOR) |
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